The Vascular Birthmarks Foundation

Dr. Linda Rozell-Shannon, PhD President and Founder

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Aliccia Braaten, United States (US), Arizona

Hello, my name is Aliccia. My 16 year old daughter Shellby was born with a venous vascular malformation in her soft pallet , cheek , and down her airway. We first found this when she was three months old and she had surgery for ear aches and placed tubes in both ears.

We were referred to Primary Children’s Hospital in Salt Lake City, Utah were she was diagnosed with a hemangioma. The doctor explained that the birthmark could be a malformation, which was confirmed when Shelly was four. She gone on to receive eleven ear tube replacements, and also has been performing sclerotherapy at the Phoenix Children’s Hospital. I try to be a solid, strong and understanding parent but I have had my sad, confused, and angry days as well. I know that my daughter is the strongest, most amazing kid I have ever had the privledge to be around. We try to find any and all information and assistance on anything associated with these birthmarks so that Shellby can live an informed life with a vascular anomaly. Thank You.